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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237814생성일: 2026년 10월 26일

4-Cyclohexylphenol → (S)-2-(4-cyclohexyl-phenoxymethyl)-7-oxo-2,3-dihydro-7H-oxazolo[3,2-a]pyrimidine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/237814

반응식

참여 물질

역할이름HCID투입량
반응물4-CyclohexylphenolHCID 14327—
반응물Diethyl acetylenedicarboxylateHCID 69803—
반응물(-)-EpichlorohydrinHCID 2734062—
반응물(S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamineHCID 66875140—
용매EthanolHCID 702—
생성물(S)-2-(4-cyclohexyl-phenoxymethyl)-7-oxo-2,3-dihydro-7H-oxazolo[3,2-a]pyrimidine-5-carboxylic acid ethyl esterHCID 2506951058.9%

반응 단계

To a solution of (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine (0.5 g, 1.82 mmol), prepared in accordance with the procedures described in Steps 1 and 2 of Example 1 and starting from R-epichlorohydrin and 4-cyclohexylphenol, in ethanol (10 mL) was added diethyl acetylenedicarboxylate (0.39 g, 2.29 mmol). The reaction mixture was heated at reflux for 14 hours and then stored in a freezer overnight. The reaction mixture was warmed to room temperature. The resulting crystalline solid was isolated by centrifugation and dried under vacuum at 60° C. to afford 427 mg of (S)-2-(4-cyclohexyl-phenoxymethyl)-7-oxo-2,3-dihydro-7H-oxazolo[3,2-a]pyrimidine-5-carboxylic acid ethyl ester. [α]D25 −16.15 (c 0.52, CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642603B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f04a2079081a4dda8d70ba64ad20b47c
출처 메모uspto-grants-2014_02